Functional Skills

Process Design / Re-engineering

Certifications

PMPProject Management Professional

Sector Experience

Healthcare
Financial Services
Business Services
Aerospace & Defense
4
jobs

Jobs Completed

1036
hours

Total Hours Logged

33
years

Years of Experience

3/19

Member Since


Fortune 500

Experience

 
Independent Consultant Management Consulting
Consultant
09/2013 - Present
Consultant specializing in clinical research processes including quality and audit, business transformation, project management and site monitoring.

IBM Life Sciences Operations
Global Regulatory Compliance Executive and Managing Consultant
03/2002 - 09/2013
Designed, sold and implemented major contracts of $1.7B, $500M, and a wide variety of smaller contracts. Directly managed a global team of 10 quality professionals overseeing staff of 2000+ executing more than 700 procedures supporting an average of two audits per month. Accountable for GxP, data privacy, and cross-border quality and compliance, continuous improvement and audit of pharmaceutical, biotech and medical device outsourced customers. Internal and external consulting projects.

CSC Health Solutions Consulting Management Consulting
Principal Consultant
05/2000 - 03/2002
Principal consultant on a wide variety of regulated projects including biotech, pharma, medical device, healthcare, and agricultural chemicals. e-Compliance practice manager and solution designer for Electronic Data Collection project.

Merck Operations
Clinical Research Associate and National Field Support
12/1993 - 05/2000
• Chair, Clinical Research Operations Technology Task Force. Accountable for global standards, implementation and support of new research technologies and platforms including Electronic Data Collection (EDC), Interactive Voice Response (IVR), Clinical Trial Management Systems (CTMS), etc.
• “Firefighter” and Trainer, accountable for the overall quality and performance of western region sites and CRAs
• CRA Certified Mentor
• Singulair product line Technical Liaison

Pharmaco-LSR Operations
Clinical Research Associate and Clinical Coordinator
04/1991 - 12/1993
• Selected to Pharmaco-LSR Advisory Board to represent Clinical Research Services to the company, providing field efficiency perspectives relating to corporate policies and procedures
• Awarded “Target 100” by Sponsor for exceptional individual achievement
• Trainer of new personnel in regulations and procedures, including training in the field
• Trainer of new personnel in Phase I procedures and regulations
• Specialist in radio-labeled trials